A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908301



Internal ID22683511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102183552..102215293hg38UCSC Ensembl
chr10:103943309..103975050hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3831742
hg1931742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908301
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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